Human Phenotype Ontology 
Grandparent Node:
Abnormal visual fixation (HP:0025404)help
Parent Node:
Eccentric visual fixation (HP:0025549)help
..Starting node
Parafoveal fixation (HP:0031768)help
Term ID: 31768
Name: Parafoveal fixation
Definition: Fixation of an object in the area adjacent to the fovea.
Reference: HP:0031768
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbsolute eccentric fixation (HP:0500072) help
..expandPeripheral fixation (HP:0031769) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031768HP:0031768Parafoveal fixation0 CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.